免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
英文原题:The Unexpected Benefit of TCR Cross-Reactivity in Cancer Immunotherapy.
The Unexpected Benefit of TCR Cross-Reactivity in Cancer Immunotherapy.
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T 细胞受体(TCR)识别肿瘤相关抗原(TAA)的能力,是过继转移TIL(肿瘤浸润淋巴细胞)T 细胞疗法发挥作用的关键驱动因素,而该疗法可以成为极其有效的癌症免疫疗法。尽管 TCR 具有交叉反应性、能够结合多种不同肽抗原是已知事实,但这一特征通常被认为不利,并被视为 TCR 疗法的局限。在近期发表于《Cell》的一篇文章中,Dolton 及其同事发现,从成功治疗黑色素瘤所用 TIL 中分离的某些 TCR 具有有益的交叉反应性,能够识别多种 TAA。此外,他们阐明了 TCR 交叉反应性在清除癌细胞方面的累积价值,以及其在靶向癌症免疫疗法中的潜在优势。
The ability of T-cell receptors (TCR) to recognize tumor-associated antigens (TAA) is a key driver of adoptive transfer of tumor-infiltrating lymphocyte (TIL) T cells, which can be a highly effective cancer immunotherapy.
While it is common knowledge that TCRs are cross-reactive and can bind multiple different peptide antigens, this is typically considered an unattractive feature and limitation for TCR-based therapies. In a recent publication in Cell, Dolton and colleagues discover that certain TCRs, isolated from TILs used for successful treatment of melanoma, possess beneficial cross-reactivity by recognizing multiple TAA.
Moreover, they elucidate the cumulative value of TCR cross-reactivity on cancer cell eradication and its prospective advantages for targeted cancer immunotherapies.
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